@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs130_head
{
this:
np:hasAssertion
dgn-np:NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs130_assertion
;
np:hasProvenance
dgn-np:NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs130_provenance
;
np:hasPublicationInfo
dgn-np:NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs130_assertion
a
np:Assertion
.
dgn-np:NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs130_provenance
a
np:Provenance
.
dgn-np:NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs130_assertion
{
miriam-gene:2067
a
ncit:C16612
.
lld:C0013336
a
ncit:C7057
.
dgn-gda:DGN0c19d01ec80b8be931e347afc059e524
sio:SIO_000628
miriam-gene:2067
,
lld:C0013336
;
a
sio:SIO_001121
.
}
dgn-np:NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs130_provenance
{
dgn-np:NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs130_assertion
dcterms:description
"[In addition to the previously reported symptoms of severe runting, abnormalities of liver nuclei and greatly reduced lifespan (which appeared less severe in the truncation mutant), both types of ERCC1-mutant mouse exhibited an absence of subcutaneous fat, early onset of ferritin deposition in the spleen, kidney malfunction, gross abnormalities of ploidy and cytoplasmic invaginations in nuclei of liver and kidney, and compromised NER and cross-link repair.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:9197240
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP188937.RAmiezFH6qxiba02-NOpzZwJxfzOV9ZOscbW4Yg8WocNs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:44+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}